(12) United States Patent (10) Patent No.: US 8,828,703 B2

(12) United States Patent (10) Patent No.: US 8,828,703 B2

USOO8828703B2 (12) UnitedO States Patent (10) Patent No.: US 8,828,703 B2 Ladner (45) Date of Patent: Sep. 9, 2014 (54) PROTEASE INHIBITION 6,423,498 B1 7/2002 Markland et al. 6,534,276 B1 3/2003 Wun et al. (75) Inventor: Robert C. Ladner, Ijamsville, MD (US) 6,583,1086,548,262 B1B2 4/20036/2003 TamburiniGentz et al. et al. (73) Assignee: Dyax Corp., Burlington, MA (US) 6,783,9606,689,582 B2B1 2/20048, 2004 E"Davies et al. 6,806,360 B2 10/2004 Wun et al. (*) Notice: Subject to any disclaimer, the term of this 6,914, 135 B2 7/2005 Sheppard et al. patent is extended or adjusted under 35 23. R: $39. E. 1 U.S.C. 154(b) by 1314 days. 2002/01W 11460 I A1 8/2002 Hollowaya ca. 2003.0114372 A1 6/2003 White et al. (21) Appl. No.: 11/646,148 2003/01296.59 A1 7, 2003 Whelihan et al. 2003/0175919 A1 9/2003 Ley et al. (22) Filed: Dec. 27, 2006 2004/0152633 A1 8/2004 Jorgensen et al. 2004/0171794 A1 9, 2004 Ladner et al. 65 Prior Publication Dat 2005, 0004021 A1 1/2005 Sprecher et al. (65) O DO 2005, 0164945 A1 7, 2005 Nixon et al. US 2008/O255O25A1 Oct. 16, 2008 2005/O180977 A1 8, 2005 Nixon et al. 2006/0264.603 A1 11/2006 Markland et al. O O 2007/002O252 A1 1/2007 Ladner et al. Related U.S. Application Data 2008/O1394.73 A1 6/2008 Ladner et al. 2009,0264350 A1 10, 2009 Blair et al. (60) gyal application No. 60/754,903, filed on Dec. 2010/0286061 A1 1 1/2010 Devy et al. FOREIGN PATENT DOCUMENTS (51) Int. Cl. CI2N 9/48 (2006.01) EP O 274 826 T 1988 CI2N IS/00 (2006.01) EP O 318 451 5, 1989 CI2P2/06 (2006.01) W8 wo3:56, 38; CI2P 2L/04 (2006.01) WO WOO1? 68.707 9, 2001 (52) U.S. Cl. WO WO 2005/021557 3, 2005 USPC .......... 435/212:435/69.1; 435/71. 1; 435/.440 OTHER PUBLICATIONS (58) Field of Classification Search USPC . 435/212, 69.1, 71.1, 440 Branden et al. Introduction to Protein Structure, Garland Publishing See application file for complete search history. Inc., New York, p. 247, 1991.* Sheffield. Modification of clearance of therapeutic and potentially (56) References Cited therapeutic proteins. Curr Drug Targets Cardiovasc Haematol U.S. PATENT DOCUMENTS Disord. Jun. 2001;1(1):1-22.* Wriggers et al. Control of protein functional dynamics by peptide 4,966,852 A 10, 1990 Wun et al. linkers Biopolymers. 2005:80(6):736-46.* 5,106,833. A 4, 1992 Broze, Jr. et al. International Search Report of International Application No. PCT/ 5,212,091 A 5, 1993 Diaz-Collier et al. US06/49322 mailed Dec. 7, 2007. 5,223,409 A 6, 1993 Ladner et al. Fries et al., Inter-alpha-inhibitor, hyaluronan and inflammation, Acta 5,312,736 A 5/1994 Rasmussen et al. Biochimica Polonica, 2003, vol. 50, No. 3, pp. 735-742. 5,378,614 A 1/1995 Petersen et al. Magkl 5,455,338 A 10/1995 Sprecher et al. agklara1-rap eta al., Characterization of the enzymaticM activity of human 5,466,783 A 11/1995 Wun et al. kallikrein 6:Autoactivation, Substrate specificity, and regulation by 5,563,123 A 10, 1996 Innis et al. inhibitors, Biochem. Biophys. Res. Commun., Aug. 2003, 5,589.359 A 12/1996 Innis et al. 8:307(4):948-55, abstract only. 5,618,696 A 4/1997 Norris et al. Scarff et al., Targeted Disruption of SP13/Serpinb6 DoesNot Result 5,629, 176 A 5/1997 Bjorn et al. in Developmental or Growth Defects, Leukocyte Dysfunction, or s A 3. 1992 di t al. Susceptibility to Stroke, Molecular and Cellular Biology, May 2004, ww- ey et al. pp. 4075-4082. s: A 3. R et al 1 Taggart et al., Inactivation of Human beta-Defensins 2 and 3 by 5,780,265- w A 7, 1998 Denniselley etet al.al. Eatolytic Cathepsins 1. TheJournal ofImmunology, 2003, 170:931* V - 5,786.328 A 7, 1998 Dennis et al. 5,795,954. A 8, 1998 Lazarus et al. 5,834,244. A 1 1/1998 Dennis et al. (Continued) 5,863,893 A 1/1999 Dennis et al. 5,880,256 A 3/1999 Dennis et al. Primary Examiner —Yong Pak 5,914,316 A 6, 1999 Brown et al. (74) Attorney, Agent, or Firm — Wolf, Greenfield & Sacks, 6,008,196 A 12/1999 Curran et al. P.C. 6,057,287 A 5, 2000 Markland et al. 6,063,764 A 5/2000 Creasey et al. 6,071,723 A 6, 2000 Markland et al. (57) ABSTRACT 6,103,500 A 8, 2000 Innis et al. Proteins including engineered sequences which inhibit pro 6,174,7216,171,587 B1 1/2001 WunInnis etet al. teases are disclosed, including proteins having two or more 6,180,607 B1 1/2001 Davies et al. engineered KunitZ domains, and uses of Such proteins. 6,242,414 B1 6/2001 Johnson et al. 6,333,402 B1 12/2001 Markland et al. 7 Claims, No Drawings US 8,828.703 B2 Page 2 (56) References Cited Mine et al., “Strutural Mechanism for Heparin-Binding of the Third Kunitz Domain of Human Tissue Factor Pathway Inhibitor.” Bio OTHER PUBLICATIONS chemistry, 41:78-85 (2002). 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